Gerd Dürner

2.2k total citations
64 papers, 1.8k citations indexed

About

Gerd Dürner is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Gerd Dürner has authored 64 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 27 papers in Molecular Biology and 11 papers in Spectroscopy. Recurrent topics in Gerd Dürner's work include Asymmetric Synthesis and Catalysis (24 papers), Synthetic Organic Chemistry Methods (21 papers) and Chemical Synthesis and Analysis (13 papers). Gerd Dürner is often cited by papers focused on Asymmetric Synthesis and Catalysis (24 papers), Synthetic Organic Chemistry Methods (21 papers) and Chemical Synthesis and Analysis (13 papers). Gerd Dürner collaborates with scholars based in Germany, United Kingdom and Austria. Gerd Dürner's co-authors include Jan W. Bats, Michael Göbel, Gerhard Quinkert, Hans‐Günther Schmalz, Olav Schiemann, Thomas F. Prisner, J. Plackmeyer, Dominik Margraf, Bela E. Bode and Michael Bolte and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Gerd Dürner

64 papers receiving 1.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gerd Dürner Germany 27 1.3k 510 222 205 201 64 1.8k
Hiroshi Suemune Japan 31 2.2k 1.7× 1.3k 2.5× 377 1.7× 445 2.2× 254 1.3× 178 2.9k
Tetsuo Iwama Japan 18 1.3k 1.0× 212 0.4× 175 0.8× 132 0.6× 131 0.7× 42 1.5k
Paul Lloyd‐Williams Spain 20 820 0.6× 659 1.3× 137 0.6× 116 0.6× 198 1.0× 43 1.4k
Andrei G. Kutateladze United States 31 1.7k 1.3× 865 1.7× 552 2.5× 101 0.5× 437 2.2× 143 2.8k
George Sosnovsky United States 21 1.2k 0.9× 331 0.6× 112 0.5× 234 1.1× 263 1.3× 120 1.8k
Xavier Creary United States 28 2.3k 1.8× 380 0.7× 303 1.4× 289 1.4× 141 0.7× 123 2.7k
Roger F. Newton United Kingdom 19 1.0k 0.8× 496 1.0× 240 1.1× 109 0.5× 118 0.6× 133 1.5k
Vinicio Zanirato Italy 23 1.5k 1.2× 592 1.2× 138 0.6× 210 1.0× 227 1.1× 78 1.9k
Javier Pérez‐Castells Spain 28 3.3k 2.5× 957 1.9× 125 0.6× 353 1.7× 143 0.7× 99 3.7k
Rudolph K. Kullnig United States 19 729 0.6× 391 0.8× 206 0.9× 146 0.7× 91 0.5× 45 1.2k

Countries citing papers authored by Gerd Dürner

Since Specialization
Citations

This map shows the geographic impact of Gerd Dürner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gerd Dürner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gerd Dürner more than expected).

Fields of papers citing papers by Gerd Dürner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerd Dürner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gerd Dürner. The network helps show where Gerd Dürner may publish in the future.

Co-authorship network of co-authors of Gerd Dürner

This figure shows the co-authorship network connecting the top 25 collaborators of Gerd Dürner. A scholar is included among the top collaborators of Gerd Dürner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gerd Dürner. Gerd Dürner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ullrich, Stefan, et al.. (2011). Cleavage of Phosphodiesters and of DNA by a Bis(guanidinium)naphthol Acting as a Metal‐Free Anion Receptor. ChemBioChem. 12(8). 1223–1229. 18 indexed citations
2.
Göbel, Michael, et al.. (2009). Synthetic Aromatic Amino Acids from a Negishi Cross-Coupling Reaction. Synthesis. 2010(2). 293–303. 4 indexed citations
3.
Dürner, Gerd, et al.. (2008). C2-symmetric bisamidines: Chiral Brønsted bases catalysing the Diels-Alder reaction of anthrones. Beilstein Journal of Organic Chemistry. 4. 28–28. 11 indexed citations
4.
Lopez, Jakob J., et al.. (2008). A practical synthesis of the 13C/15N-labelled tripeptide N-formyl-Met-Leu-Phe, useful as a reference in solid-state NMR spectroscopy. Beilstein Journal of Organic Chemistry. 4. 35–35. 2 indexed citations
5.
Krebs, Andreas, Ursula Dietrich, Jan Ferner, et al.. (2007). Tripeptides from Synthetic Amino Acids Block the Tat–TAR Association and Slow Down HIV Spread in Cell Cultures. ChemBioChem. 8(15). 1850–1856. 15 indexed citations
6.
Dürner, Gerd, et al.. (2007). Synthesis of C2-Symmetric Bisamidines:  A New Type of Chiral Metal-Free Lewis Acid Analogue Interacting with Carbonyl Groups. The Journal of Organic Chemistry. 72(15). 5618–5624. 46 indexed citations
7.
Krebs, Andreas, et al.. (2004). Enantioselective Synthesis of Non‐Natural Aromatic α‐Amino Acids. Chemistry - A European Journal. 10(2). 544–553. 37 indexed citations
8.
Ding, Li, Kuangbiao Ma, Gerd Dürner, et al.. (2002). Reactions of ferrocenylboranes with 2,5-bis(pyridyl)pyrazine and quaterpyridine: charge-transfer complexes and redox-active macrocycles. Journal of the Chemical Society Dalton Transactions. 1566–1573. 45 indexed citations
9.
Mulzer, Johann, Gerd Dürner, & Dirk Trauner. (1996). Formale Totalsynthese von (−)‐Morphin über konjugierte Cuprataddition. Angewandte Chemie. 108(23-24). 3046–3048. 15 indexed citations
10.
11.
Quinkert, Gerhard, et al.. (1992). Photolactamization: A Novel Synthetic Entry into Large Ring-Sized Lactams. Tetrahedron Letters. 33(15). 1977–1980. 10 indexed citations
12.
Quinkert, Gerhard, et al.. (1992). An enantioselective version of the AB+B→ABCD-type steroid total synthesis. Tetrahedron Letters. 33(25). 3617–3620. 41 indexed citations
13.
Quinkert, Gerhard, et al.. (1992). Enantioselective Conjugate Addition Greatly Improves the Synthesis of (+)-Confertin. Tetrahedron Letters. 33(24). 3469–3472. 21 indexed citations
14.
Quinkert, Gerhard, H. Peter Nestler, Heinrich Becker, et al.. (1990). Weitere Beiträge zur Synthese von (+)‐Aspicilin. Helvetica Chimica Acta. 73(7). 1999–2047. 12 indexed citations
15.
Quinkert, Gerhard, et al.. (1988). Synthese des Flechtenmakrolids (+)‐Aspicilin mit Photolactonisierung als Schlüsselreaktion. Helvetica Chimica Acta. 71(7). 1719–1794. 30 indexed citations
16.
Quinkert, Gerhard, Klaus R. Schmieder, Jan W. Bats, et al.. (1986). Über Dienketene aus o‐Chinolacetaten. Helvetica Chimica Acta. 69(3). 469–537. 22 indexed citations
17.
Quinkert, Gerhard, et al.. (1982). Asymmetrische Totalsynthese von 19‐Nor‐Steroiden mit photochemischer Schlüsselreaktion: Enantiomerenreine Zielverbindungen. Liebigs Annalen der Chemie. 1982(11). 1999–2040. 43 indexed citations
18.
Quinkert, Gerhard, et al.. (1981). Hochselektive Totalsynthese von 19‐Nor‐Steroiden mit photochemischer Schlüsselreaktion: Racemische Zielverbindungen1,4). Liebigs Annalen der Chemie. 1981(12). 2335–2371. 27 indexed citations
19.
Quinkert, Gerhard, et al.. (1980). A Photochemical Route to (7±)‐Estrone. Angewandte Chemie International Edition in English. 19(12). 1027–1029. 28 indexed citations
20.
Quinkert, Gerhard, et al.. (1980). Ein photochemischer Weg zu (±)-östron. Angewandte Chemie. 92(12). 1060–1062. 14 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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